"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1170298	NM_001256864.2(DNAJC6):c.544-9C>T	DNAJC6	Single nucleotide variant (intron variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 474681	NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign/Likely benign
Select item 1170299	NM_001256864.2(DNAJC6):c.1500G>A (p.Glu500=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1167136	NM_001256864.2(DNAJC6):c.1506C>T (p.His502=)	DNAJC6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1167137	NM_001256864.2(DNAJC6):c.1983T>C (p.Ser661=)	DNAJC6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1170300	NM_001256864.2(DNAJC6):c.2010A>C (p.Pro670=)	DNAJC6	Single nucleotide variant (synonymous variant)	Juvenile onset Parkinson disease 19A +1 more	GBenign
Select item 1167138	NM_001256864.2(DNAJC6):c.2183G>A (p.Ser728Asn)	DNAJC6 (S658N +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign

ClinVar